TY - JOUR
T1 - Heterogeneity in human cardiac troponin I standards
AU - Bunk, David M.
AU - Dalluge, Joseph J.
AU - Welch, Michael J.
PY - 2000/9/10
Y1 - 2000/9/10
N2 - The LC-MS analysis of recombinant cardiac troponin I (cTnI) and cTnI extracted from human hearts showed a high degree of structural heterogeneity among all samples. The examined recombinant cTnI samples indicated posttranslational modifications, presumably due to their purification (i.e., 2-mercaptoethanol adducts and carbamylation) and related to their expression (i.e., an N-terminal expression tag). The extracted cTnI samples, while having a higher degree of structural heterogeneity, showed less structural variance between samples than the recombinant proteins. The LC-MS analysis of the extracted cTnI samples provided evidence of posttranslational modification by phosphorylation, acetylation, proteolytic cleavage, and intrachain disulfide bond formation.
AB - The LC-MS analysis of recombinant cardiac troponin I (cTnI) and cTnI extracted from human hearts showed a high degree of structural heterogeneity among all samples. The examined recombinant cTnI samples indicated posttranslational modifications, presumably due to their purification (i.e., 2-mercaptoethanol adducts and carbamylation) and related to their expression (i.e., an N-terminal expression tag). The extracted cTnI samples, while having a higher degree of structural heterogeneity, showed less structural variance between samples than the recombinant proteins. The LC-MS analysis of the extracted cTnI samples provided evidence of posttranslational modification by phosphorylation, acetylation, proteolytic cleavage, and intrachain disulfide bond formation.
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U2 - 10.1006/abio.2000.4710
DO - 10.1006/abio.2000.4710
M3 - Article
C2 - 10964401
AN - SCOPUS:0034633280
SN - 0003-2697
VL - 284
SP - 191
EP - 200
JO - Analytical Biochemistry
JF - Analytical Biochemistry
IS - 2
ER -